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Beijing Tide Pharmaceutical Co., Ltd.
  • Founded in:

    1995-05-29
  • Country:

    China China
  • Address:

    No. 8 Rongjing East Street, Beijing Economic and Technological Development Zone, Beijing
  • Tax NO.:

    911103026000314683
  • Registered Funds:

    500 million yuan
  • Website:

  • Email:

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Beraprost Sodium Tablets
The main ingredient of this product is beraprost sodium, and its chemical name is: (±)-2,3,3a,8b-tetrahydro-2-hydroxy-1-(3-hydroxy-4-methyl-1-octen-6-ynyl)-1H-cyclopenta[b]benzofuran-5-butyric acid sodium
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Beraprost sodium

This product is a derivative of prostacyclin (PGI2) with strong antiplatelet aggregation and vasodilation effects. It is a prostacyclin derivative that can be taken orally, with strong vasodilation and antiplatelet aggregation effects.

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Alprostadil Injection
Prostaglandin E1. Excipients: refined soybean oil, refined lecithin, concentrated glycerol, oleic acid, sodium hydroxide, water for injection.
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Prostaglandin E1

Dilate blood vessels, inhibit platelet aggregation; stabilize liver cell membranes and improve liver function

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Alprostadil Injection
The main ingredient is alprostadil. Its chemical name is (1R, 2R, 3R)-3-hydroxy-2[(E)-(3S)-3-hydroxy-1-octenyl]-5-oxocyclopentaneheptanoic acid. Molecular formula: C20H34O5. Molecular weight: 354.49.
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Prostaglandin E1

This product is an intravenous alprostadil preparation with lipid microspheres as drug carriers. Due to the encapsulation of lipid microspheres, alprostadil is not easy to be inactivated. In addition, this product has the targeting characteristics of being easily distributed to damaged blood vessels, thereby exerting the effects of this product in dilating blood vessels and inhibiting platelet aggregation.

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This product is an intravenous alprostadil preparation with lipid microspheres as drug carriers. Due to the encapsulation of lipid microspheres, alprostadil is not easy to be inactivated. In addition, this product has the targeting characteristics of being easily distributed to damaged blood vessels, thereby exerting the effects of this product in dilating blood vessels and inhibiting platelet aggregation.

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Pioglitazone Hydrochloride Dispersible Tablets
Pioglitazone hydrochloride. Molecular weight: C19H20N2O3S·HCl
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Pioglitazone hydrochloride

This product belongs to the class of thiazolidinediones oral antidiabetic drugs, and is a highly selective peroxisome proliferator-activated receptor γ (PPARγ) agonist, which controls blood sugar levels by increasing peripheral and liver insulin sensitivity. Its main mechanism of action is to activate PPARγ nuclear receptors in tissues such as fat, skeletal muscle and liver where insulin acts, thereby regulating the transcription of insulin-responsive genes and controlling the generation, transport and utilization of blood sugar.

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This product belongs to the class of thiazolidinediones oral antidiabetic drugs, and is a highly selective peroxisome proliferator-activated receptor γ (PPARγ) agonist, which controls blood sugar levels by increasing peripheral and liver insulin sensitivity. Its main mechanism of action is to activate PPARγ nuclear receptors in tissues such as fat, skeletal muscle and liver where insulin acts, thereby regulating the transcription of insulin-responsive genes and controlling the generation, transport and utilization of blood sugar.

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Limaprost Tablets
The active ingredient is limaprost
Name Description Content CAS NO. Registered Holders
LIMAPROST

Unspecified

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Unspecified

74397-12-9 1
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